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Screening of novel restless legs syndrome–associated genes in French-Canadian families
OBJECTIVE: To examine whether any rare, protein-altering variants could be identified across 13 recently identified restless legs syndrome (RLS) loci in familial French-Canadian cases. METHODS: Whole-exome sequences from 7 large French-Canadian families (4–8 affected per family for a total of 38 cas...
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| Publicado en: | Neurol Genet |
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| Autores principales: | , , , , , |
| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
Wolters Kluwer
2018
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| Materias: | |
| Acceso en línea: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6305992/ https://ncbi.nlm.nih.gov/pubmed/30637332 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1212/NXG.0000000000000296 |
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